Nonaka I - Search Results

1

Effects of enzyme replacement therapy on five patients with advanced late-onset glycogen storage disease type II: a 2-year follow-up study.

Furusawa Y, Mori-Yoshimura M, Yamamoto T, Sakamoto C, Wakita M, Kobayashi Y, Fukumoto Y, Oya Y, Fukuda T, Sugie H, Hayashi YK, Nishino I, Nonaka I, Murata M. Furusawa Y, et al. Among authors: nonaka i. J Inherit Metab Dis. 2012 Mar;35(2):301-10. doi: 10.1007/s10545-011-9393-6. Epub 2011 Oct 7. J Inherit Metab Dis. 2012. PMID: 21984055

2

A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom.

Kinoshita H, Goto Y, Ishikawa M, Uemura T, Matsumoto K, Hayashi YK, Arahata K, Nonaka I. Kinoshita H, et al. Among authors: nonaka i. Brain Dev. 1995 May-Jun;17(3):202-5. doi: 10.1016/0387-7604(95)00018-7. Brain Dev. 1995. PMID: 7573761 Review.

3

Deficiency of laminin alpha 2-chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy.

Hayashi YK, Koga R, Tsukahara T, Ishii H, Matsuishi T, Yamashita Y, Nonaka I, Arahata K. Hayashi YK, et al. Among authors: nonaka i. Muscle Nerve. 1995 Sep;18(9):1027-30. doi: 10.1002/mus.880180918. Muscle Nerve. 1995. PMID: 7643867 No abstract available.

4

Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation.

Sugie H, Sugie Y, Ito M, Fukuda T, Nonaka I, Igarashi Y. Sugie H, et al. Among authors: nonaka i. Clin Chim Acta. 1995 Apr 30;236(1):81-6. doi: 10.1016/0009-8981(95)06044-x. Clin Chim Acta. 1995. PMID: 7664468

5

The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin.

Hayashi YK, Mizuno Y, Yoshida M, Nonaka I, Ozawa E, Arahata K. Hayashi YK, et al. Among authors: nonaka i. Neurology. 1995 Mar;45(3 Pt 1):551-4. doi: 10.1212/wnl.45.3.551. Neurology. 1995. PMID: 7898714

6

Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle.

Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Suzuki A, Hagiwara Y, Hayashi YK, Arahata K, Nonaka I, Hirai S, et al. Mizuno Y, et al. Among authors: nonaka i. Biochem Biophys Res Commun. 1994 Sep 15;203(2):979-83. doi: 10.1006/bbrc.1994.2278. Biochem Biophys Res Commun. 1994. PMID: 8093083

7

Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive form.

Kobayashi O, Hayashi Y, Arahata K, Ozawa E, Nonaka I. Kobayashi O, et al. Among authors: nonaka i. Neurology. 1996 Mar;46(3):815-8. doi: 10.1212/wnl.46.3.815. Neurology. 1996. PMID: 8618689

8

Detection of DNA fragments encompassing the deletion junction of mitochondrial genome.

Goto Y, Nishino I, Horai S, Nonaka I. Goto Y, et al. Among authors: nonaka i. Biochem Biophys Res Commun. 1996 May 15;222(2):215-9. doi: 10.1006/bbrc.1996.0724. Biochem Biophys Res Commun. 1996. PMID: 8670185

9

Cerebral oxygen and glucose metabolism in glycogen storage disease with normal acid maltase: case report.

Katsumi Y, Fukuyama H, Ogawa M, Matsui M, Tokonami F, Aii H, Sugie H, Murakami N, Nonaka I. Katsumi Y, et al. Among authors: nonaka i. J Neurol Sci. 1996 Sep 1;140(1-2):46-52. doi: 10.1016/0022-510x(96)00077-9. J Neurol Sci. 1996. PMID: 8866426

10

The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).

Nishino I, Komatsu M, Kodama S, Horai S, Nonaka I, Goto Y. Nishino I, et al. Among authors: nonaka i. Muscle Nerve. 1996 Dec;19(12):1603-4. doi: 10.1002/(SICI)1097-4598(199612)19:12<1603::AID-MUS10>3.0.CO;2-S. Muscle Nerve. 1996. PMID: 8941275 No abstract available.

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